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    Specialist - QA Ops - Manufacturing Mgmt

    REQ-10041624
    2月 24, 2025
    Singapore

    摘要

    This role support/provide quality oversight in ensuring a smooth manufacturing operation, new product launches/transfer in a compliant/timely manner, drug substance batch review/release are in full gmp compliance to regulatory standards and ensures quality strategy/continuous improvement are driven in alignment to site objective/s.

    About the Role

    Key Responsibilities:

    • Ensure all activities in compliance with cGxP, incl. data integrity
    • Review and approval of analytical data / tests (analytical release)
    • Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance
    • Support exception investigations
    • Review and approval of production, QC, and AS & T records
    • MBR review. Support OpEx improvement projects. Executes batch release in compliance with registration (if Qualified Person)
    • Comply with all HSE guidelines. Detect and report potential accident, risks and propose solutions
    • Participate in HSE risk assessments. Preparation and participation to internal HSE audits

    Role Requirements :

    Essential Requirements:

    • 3+ years of experience in pharmaceutical quality control, quality assurance or production
    • Operations Management and Execution; Functional Breadth; Collaborating across boundaries; Applied Practice
    • Collaboration; result-oriented. Good knowledge of GMP; Continuous Learning; Operational Excellence; Digital & Tech Savvy
    • MS Office applications and other standard IT applications supporting Quality activities
    • Technological competence; Quality Assurance; Knowledge of GMP, Quality Standards; Quality Control (QC) Testing

    Desirable Requirements:
    • University degree with a scientific / technological background (e.g. Chemistry, Pharmacy, Biology, Biochemistry, or equivalent)

    Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

    Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

    Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

    Operations
    Innovative Medicines
    Singapore
    Tuas South Avenue
    Quality
    Full time
    Regular
    No

    Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

    A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
    REQ-10041624

    Specialist - QA Ops - Manufacturing Mgmt

    Apply to Job

    Source URL: https://www.bkartpay.com/careers/career-search/job/details/req-10041624-specialist-qa-ops-manufacturing-mgmt

    List of links present in page
    1. https://www.novartis.com/about/strategy/people-and-culture
    2. https://talentnetwork.novartis.com/network
    3. https://www.novartis.com/careers/benefits-rewards
    4. https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Tuas-South-Avenue/Specialist---QA-Ops---Manufacturing-Mgmt_REQ-10041624
    5. https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Tuas-South-Avenue/Specialist---QA-Ops---Manufacturing-Mgmt_REQ-10041624